Salivary flow rate and biochemical composition analysis in stimulated whole saliva of children with cystic fibrosis

A rapid and sensitive method for the quantitation of microgram quantities of protein utilizing the principle of protein-dye binding

Bradford, M. M. (1976) · Analytical Biochemistry · doi:10.1016/0003-2697(76)90527-3 · Cited by 255,302 · see citing works

Cystic fibrosis genetics: from molecular understanding to clinical application

Cutting, G. R. (2014) · Nature Reviews Genetics · doi:10.1038/nrg3849 · Cited by 969 · see citing works

Regulation of salivary gland function by autonomic nerves.

Proctor, G., & Carpenter, G. (2007) · Autonomic Neuroscience: Basic & Clinical · doi:10.1016/j.autneu.2006.10.006 · Cited by 723 · see citing works

Cystic fibrosis mortality and survival in the UK: 1947–2003

DODGE, J. A., Lewis, P. A., Stanton, M., & Wilsher, J. (2006) · European Respiratory Journal · doi:10.1183/09031936.00099506 · Cited by 627 · see citing works

Cystic fibrosis: a disease in electrolyte transport

Quinton, P. (1990) · The FASEB Journal · doi:10.1096/fasebj.4.10.2197151 · Cited by 507 · see citing works

Standards of care for patients with cystic fibrosis: a European consensus

Kerem, E., Conway, S., Elborn, J. S., & Heijerman, H. G. M. (2005) · Journal of Cystic Fibrosis · doi:10.1016/j.jcf.2004.12.002 · Cited by 477 · see citing works

A Novel Host Defense System of Airways is Defective in Cystic Fibrosis

Moskwa, P., Lorentzen, D., Excoffon, K. J. D. A., Zabner, J., McCray, P. B., Nauseef, W. M., Dupuy, C., & Bánfi, B. (2006) · American Journal of Respiratory and Critical Care Medicine · doi:10.1164/rccm.200607-1029oc · Cited by 277 · see citing works

Salivary α-Amylase: Role in Dental Plaque and Caries Formation

Scannapieco, F. A., Torres, G., & Levine, M. J. (1993) · Critical Reviews in Oral Biology & Medicine · doi:10.1177/10454411930040030701 · Cited by 272 · see citing works

Stable thiobarbituric acid chromophore with dimethyl sulphoxide. Application to sialic acid assay in analytical de-O-acetylation

Skoza, L., & Mohos, S. C. (1976) · Biochemical Journal · doi:10.1042/bj1590457 · Cited by 267 · see citing works

Factors Influencing Outcomes in Cystic Fibrosis

Johnson, C. A., Butler, S. M., Konstan, M. W., Morgan, W. J., & Wohl, M. E. B. (2003) · CHEST Journal · doi:10.1378/chest.123.1.20 · Cited by 226 · see citing works

Origin, structure, and biological activities of peroxidases in human saliva

Ihalin, R., Loimaranta, V., & Tenovuo, J. O. (2005) · Archives of Biochemistry and Biophysics · doi:10.1016/j.abb.2005.07.004 · Cited by 203 · see citing works

Structure and biosynthesis of human salivary mucins.

Zalewska, A., Zwierz, K., Zółkowski, K., & Gindzieński, A. (2000) · Acta Biochimica Polonica · doi:10.18388/abp.2000_3960 · Cited by 142 · see citing works

Current concepts of the structure and nature of mammalian salivary mucous glycoproteins

Herp, A., Wu, A. M., & Moschera, J. A. (1979) · Molecular and Cellular Biochemistry · doi:10.1007/bf00226677 · Cited by 134 · see citing works

Evidence against Defective -Golgi Acidification in Cystic Fibrosis

Seksek, O., Biwersi, J., & Verkman, A. S. (1996) · Journal of Biological Chemistry · doi:10.1074/jbc.271.26.15542 · Cited by 95 · see citing works

Culture-based diagnostic microbiology in cystic fibrosis: Can we simplify the complexity?

Burns, J. L., & Rolain, J. (2013) · Journal of Cystic Fibrosis · doi:10.1016/j.jcf.2013.09.004 · Cited by 87 · see citing works

Antimicrobial Agents in Saliva—Protection for the Whole Body

Tenovuo, J. O. (2002) · Journal of Dental Research · doi:10.1177/154405910208101202 · Cited by 82 · see citing works

Oral health and related factors in cystic fibrosis and other chronic respiratory disorders

Narang, A. (2003) · Archives of Disease in Childhood · doi:10.1136/adc.88.8.702 · Cited by 81 · see citing works

Saliva as a potential tool for cystic fibrosis diagnosis

Gonçalves, A. C., Marson, F. A. L., de Mendonça, R. M. H., Ribeiro, J. D., Ribeiro, A. F., Paschoal, I. A., & Levy, C. E. (2013) · Diagnostic Pathology · doi:10.1186/1746-1596-8-46 · Cited by 71 · see citing works

Identification of Porphyromonas gingivalis lipopolysaccharide-binding proteins in human saliva

Choi, S., Baik, J. E., Jeon, J. H., Cho, K., Seo, D., Kum, K., Yun, C., & Han, S. H. (2011) · Molecular Immunology · doi:10.1016/j.molimm.2011.06.434 · Cited by 52 · see citing works

An observational study of matrix metalloproteinase (MMP)-9 in cystic fibrosis

Devereux, G. S., Steele, S., Jagelman, T., et al. (2014) · Journal of Cystic Fibrosis · doi:10.1016/j.jcf.2014.01.010 · Cited by 52 · see citing works

The relationship between MMPs and pH in whole saliva of radiated head and neck cancer patients

Vuotila, T., Ylikontiola, L. P., Sorsa, T. A., Luoto, H., Hanemaaijer, R., Salo, T. A., & Tjäderhane, L. (2002) · Journal of Oral Pathology and Medicine · doi:10.1034/j.1600-0714.2002.310603.x · Cited by 50 · see citing works

Thiocyanate concentration in saliva of cystic fibrosis patients.

Minarowski, Ł., Sands, D., Minarowska, A., et al. (2008) · Folia Histochemica et Cytobiologica · doi:10.2478/v10042-008-0037-0 · Cited by 48 · see citing works

Increased Oxidative Stress Induces Apoptosis in Human Cystic Fibrosis Cells

Rottner, M., Tual‐Chalot, S., Mostefai, H. A., Andriantsitohaina, R., Freyssinet, J., & Martínez, M. C. (2011) · PLoS ONE · doi:10.1371/journal.pone.0024880 · Cited by 43 · see citing works

Cystic Fibrosis

Grody, W. W. (1999) · Archives of Pathology & Laboratory Medicine · doi:10.5858/1999-123-1041-cf · Cited by 42 · see citing works

Parotid Gland Function in Children with Cystic Fibrosis and Child Control Subjects

Blomfield, J., Rush, A. R., Allars, H. M., & Brown, J. M. (1976) · Pediatric Research · doi:10.1203/00006450-197606000-00004 · Cited by 40 · see citing works

CFTR Is Involved in the Fine Tuning of Intracellular Redox Status

Duranton, C., Rubera, I., Cougnon, M., Mélis, N., Chargui, A., Mograbi, B., & Tauc, M. (2012) · American Journal Of Pathology · doi:10.1016/j.ajpath.2012.06.017 · Cited by 38 · see citing works

Clinical Science

Kinirons, M. J. (1983) · Journal of Dental Research · doi:10.1177/00220345830620070801 · Cited by 38 · see citing works

Peroxidase release from rat submandibular salivary acinar cells in vitro

Anderson, L. C. (1986) · Archives of Oral Biology · doi:10.1016/0003-9969(86)90027-0 · Cited by 37 · see citing works

Presence of developmental defects of enamel in cystic fibrosis patients.

Azevedo, T. D. P. L., Feijó, G. C. S., & Bezerra, A. C. B. (2007) · PubMed · Cited by 37 · see citing works

Clinical oral and salivary parameters of children with juvenile idiopathic arthritis

de Melo, A. R. F., de Souza, A. F., Perestrelo, B. D. O., et al. (2013) · Oral Surgery Oral Medicine Oral Pathology and Oral Radiology · doi:10.1016/j.oooo.2013.08.024 · Cited by 36 · see citing works

Saliva as a potential diagnostic tool

Deepa, T., & Thirrunavukkarasu, N. (2010) · Indian Journal of Medical Sciences · doi:10.4103/0019-5359.99854 · Cited by 36 · see citing works

Differences in the regulatory mechanism of amylase release by rat parotid and submandibular glands

Busch, L., Sterin‐Borda, L., & Borda, E. (2002) · Archives of Oral Biology · doi:10.1016/s0003-9969(02)00057-2 · Cited by 36 · see citing works

Proteomic Analysis of Nasal Epithelial Cells from Cystic Fibrosis Patients

Jeanson, L., Guerrera, I. C., Papon, J., Chhuon, C., Zadigue, P., Prulière-Escabasse, V., Amselem, S., Escudier, E. F., Coste, A., & Edelman, A. (2014) · PLoS ONE · doi:10.1371/journal.pone.0108671 · Cited by 28 · see citing works

Prostaglandins E2 and E2 alpha are elevated in saliva of cystic fibrosis patients.

Rigas, B., Korenberg, J. R., Merrill, W. W., & Levine, L. (1989) · PubMed · Cited by 28 · see citing works

Distribution of Cystic Fibrosis Transmembrane Conductance Regulator (CFTR) Mutations in a Cohort of Patients Residing in Palestine

Siryani, I., Jama, M., Rumman, N., et al. (2015) · PLoS ONE · doi:10.1371/journal.pone.0133890 · Cited by 24 · see citing works

Stimulation of salivary secretion in vivo by CFTR potentiators in Cftr+/+ and Cftr−/− mice

Noël, S., Strale, P., Dannhoffer, L., et al. (2007) · Journal of Cystic Fibrosis · doi:10.1016/j.jcf.2007.06.005 · Cited by 17 · see citing works

Modification of the salivary secretion assay in F508del mice — The murine equivalent of the human sweat test

Droebner, K., & Sandner, P. (2013) · Journal of Cystic Fibrosis · doi:10.1016/j.jcf.2013.05.001 · Cited by 14 · see citing works

Plasma biomarkers and cystic fibrosis lung disease

Cantin, A. M., Bilodeau, G., Larivée, P., et al. (2012) · Clinical and investigative medicine · doi:10.25011/cim.v35i4.17145 · Cited by 13 · see citing works

Expression of ΔF508 Cystic Fibrosis Transmembrane Regulator (CFTR) Decreases Membrane Sialylation

Dosanjh, A., & Muchmore, E. A. (2009) · The Open Respiratory Medicine Journal · doi:10.2174/1874306400903010079 · Cited by 10 · see citing works

Enterosalivary nitrate metabolism and the microbiome: Intersection of microbial metabolism, nitric oxide and diet in cardiac and pulmonary vascular health

Koch, C. D., Gladwin, M. T., Freeman, B. A., Lundberg, J. O., Weitzberg, E., & Morris, A. (2017) · Free Radical Biology and Medicine · doi:10.1016/j.freeradbiomed.2016.12.015 · Cited by 186 · see citing works

68 The physiological state of Pseudomonas aeruginosa populations in lungs of Cystic Fibrosis (CF) patients

Yang, L., Johansen, H., Haagensen, J. A. J., et al. (2006) · Journal of Cystic Fibrosis · doi:10.1016/s1569-1993(06)80059-7

40 Longitudinal values of sweat chloride concentration among infants identified by cystic fibrosis (CF) newborn screening (NBS) in California

Zirbes, J. M., Hardy, K., Sudhakar, R., et al. (2013) · Journal of Cystic Fibrosis · doi:10.1016/s1569-1993(13)60183-6

302 Comparison of airway clearance techniques (ACT) in the cystic fibrosis (CF) population: a single case study report

Forster, E., Swingwood, E. L., Nicholas, B., et al. (2014) · Journal of Cystic Fibrosis · doi:10.1016/s1569-1993(14)60437-9 · Cited by 1 · see citing works

156 Exercise performance in children with mild cystic fibrosis (CF): Are there arguments to enhance physical activity?

Keyzer, M., Cornette, J., Pyl, F., et al. (2015) · Journal of Cystic Fibrosis · doi:10.1016/s1569-1993(15)30333-7

484 Usage trends, attitudes, and barriers to airway clearance in children with cystic fibrosis

Onge, I. S., Akhtar, S., Longtine, J., et al. (2023) · Journal of Cystic Fibrosis · doi:10.1016/s1569-1993(23)01409-1